A conserved motif flags acyl carrier proteins for β-branching in polyketide synthesis.

نویسندگان

  • Anthony S Haines
  • Xu Dong
  • Zhongshu Song
  • Rohit Farmer
  • Christopher Williams
  • Joanne Hothersall
  • Eliza Płoskoń
  • Pakorn Wattana-Amorn
  • Elton R Stephens
  • Erika Yamada
  • Rachel Gurney
  • Yuiko Takebayashi
  • Joleen Masschelein
  • Russell J Cox
  • Rob Lavigne
  • Christine L Willis
  • Thomas J Simpson
  • John Crosby
  • Peter J Winn
  • Christopher M Thomas
  • Matthew P Crump
چکیده

Type I polyketide synthases often use programmed β-branching, via enzymes of a 'hydroxymethylglutaryl-CoA synthase (HCS) cassette', to incorporate various side chains at the second carbon from the terminal carboxylic acid of growing polyketide backbones. We identified a strong sequence motif in acyl carrier proteins (ACPs) where β-branching is known to occur. Substituting ACPs confirmed a correlation of ACP type with β-branching specificity. Although these ACPs often occur in tandem, NMR analysis of tandem β-branching ACPs indicated no ACP-ACP synergistic effects and revealed that the conserved sequence motif forms an internal core rather than an exposed patch. Modeling and mutagenesis identified ACP helix III as a probable anchor point of the ACP-HCS complex whose position is determined by the core. Mutating the core affects ACP functionality, whereas ACP-HCS interface substitutions modulate system specificity. Our method for predicting β-carbon branching expands the potential for engineering new polyketides and lays a basis for determining specificity rules.

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عنوان ژورنال:
  • Nature chemical biology

دوره 9 11  شماره 

صفحات  -

تاریخ انتشار 2013